An investigation of genetic and epigenetic factors in the regulation of gene expression in schizophrenia: insights into pathways involved in pathogenesis
Author(s)
Perez - Becerril, Cristina Margarita
Type
Thesis or dissertation
Abstract
Schizophrenia is a common psychiatric disorder with a complex aetiology that has a
strong genetic component as well as a major contribution from non-genetic factors.
Whilst GWAS studies have not yielded substantial evidence of DNA variants linked to
schizophrenia, microarray expression studies, which reflect both genetic and
environmental factors, have provided evidence of candidate genes whose expression
changes significantly in schizophrenia. The present thesis is based on a prospective
microarray study carried out on two brain regions implicated in schizophrenia: frontal
cortex and superior temporal cortex (Maycox et al., 2009; Barnes et al., 2011). SNP
variants in six of these genes were genotyped and allele, genotype and haplotype
analysis carried out initially to investigate associations with levels of expression found
in these microarray studies. Subsequently SNP associations with disease were
investigated in an extended case-control cohort from the East UK region. The
selected candidates genes, highlighted from microarray studies, reflected two main
functional categories: synaptic plasticity and the Wnt signalling pathway. Initial
ANOVA revealed a significant interaction of disease status with genotype/haplotype
in ZnT3 with respect to levels of expression. Significant effects of specific genotypes
and haplotypes in CACNA1E and FRZB on expression were also observed.
Furthermore, ZnT3 was the gene for which the strongest evidence of association
with schizophrenia was obtained in the East UK cohort, with four SNPs associated at
the allelic and genotypic level. Significant associations of a number of haplotypes of
ZnT3 with disease status were also identified. In addition, modest evidence of
statistical epistasis between genes within both functional groups was identified.
Finally, a method for analysis of CpG island methylation was developed based on bisulphite sequencing and methylation specific PCR (MSP) using previously validated
primers for DKK3 (Yue et al., 2008). Although DKK3 showed a low density of
methylation, the application of this method may prove useful for other candidate
genes.
strong genetic component as well as a major contribution from non-genetic factors.
Whilst GWAS studies have not yielded substantial evidence of DNA variants linked to
schizophrenia, microarray expression studies, which reflect both genetic and
environmental factors, have provided evidence of candidate genes whose expression
changes significantly in schizophrenia. The present thesis is based on a prospective
microarray study carried out on two brain regions implicated in schizophrenia: frontal
cortex and superior temporal cortex (Maycox et al., 2009; Barnes et al., 2011). SNP
variants in six of these genes were genotyped and allele, genotype and haplotype
analysis carried out initially to investigate associations with levels of expression found
in these microarray studies. Subsequently SNP associations with disease were
investigated in an extended case-control cohort from the East UK region. The
selected candidates genes, highlighted from microarray studies, reflected two main
functional categories: synaptic plasticity and the Wnt signalling pathway. Initial
ANOVA revealed a significant interaction of disease status with genotype/haplotype
in ZnT3 with respect to levels of expression. Significant effects of specific genotypes
and haplotypes in CACNA1E and FRZB on expression were also observed.
Furthermore, ZnT3 was the gene for which the strongest evidence of association
with schizophrenia was obtained in the East UK cohort, with four SNPs associated at
the allelic and genotypic level. Significant associations of a number of haplotypes of
ZnT3 with disease status were also identified. In addition, modest evidence of
statistical epistasis between genes within both functional groups was identified.
Finally, a method for analysis of CpG island methylation was developed based on bisulphite sequencing and methylation specific PCR (MSP) using previously validated
primers for DKK3 (Yue et al., 2008). Although DKK3 showed a low density of
methylation, the application of this method may prove useful for other candidate
genes.
Date Issued
2011
Date Awarded
2012-01
Advisor
de Belleroche, Jackie
Creator
Perez - Becerril, Cristina Margarita
Publisher Department
Medicine
Publisher Institution
Imperial College London
Qualification Level
Doctoral
Qualification Name
Doctor of Philosophy (PhD)